Guest guest Posted March 10, 2008 Report Share Posted March 10, 2008 Hello , My left arm has a muscle that snaps sometimes. It hurts. I think for me at least it's the Myofascial pain syndrome. Have you looked into that? SOmetimes the fascia can become hard and kind of bind the muscles in to a certain position, then when you move the muscle, it seems to snap it... gentle hugs, Loretta > > Hi all, > Has anyone experienced this weird thing: sometimes when I turn the > muscles in the front of my thighs feel almost like they snap and the > pain when this happens is excruciating. Also, my symptoms seem to be a > bit more pronounced on one side of my body than the other...is this > unheard of???? My sister in law has MS and she said my symptoms sounded > like hers before she was diagnosed. I was like " gee, thanks!! " . > Thanks for any input. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2008 Report Share Posted March 11, 2008 that would explain why my legs are sounding like they are snapping together alot. i hear it in my hips where the legs connect. i also have myofacial pain syndrome. Hugs krystal Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2008 Report Share Posted March 11, 2008 Krystal, I was just diagnosed with myofacial pain syndrome. Is there anything you can tell me about it? The Neorologist says it is pretty serious, but the Orthopedic I am seeing didnt' seem to think it all that bad. I know that I am in alot of pain in my shoulder neck and right side of my face and head. Are you on disability? Re: Snapping muscles????!!!! that would explain why my legs are sounding like they are snapping together alot. i hear it in my hips where the legs connect. i also have myofacial pain syndrome. Hugs krystal <!-- #ygrp-mkp{ border:1px solid #d8d8d8;font-family:Arial;margin:14px 0px;padding:0px 14px;} #ygrp-mkp hr{ border:1px solid #d8d8d8;} #ygrp-mkp #hd{ color:#628c2a;font-size:85%;font-weight:bold;line-height:122%;margin:10px 0px;} #ygrp-mkp #ads{ margin-bottom:10px;} #ygrp-mkp .ad{ padding:0 0;} #ygrp-mkp .ad a{ color:#0000ff;text-decoration:none;} --> <!-- #ygrp-sponsor #ygrp-lc{ font-family:Arial;} #ygrp-sponsor #ygrp-lc #hd{ margin:10px 0px;font-weight:bold;font-size:78%;line-height:122%;} #ygrp-sponsor #ygrp-lc .ad{ margin-bottom:10px;padding:0 0;} --> <!-- #ygrp-mlmsg {font-size:13px;font-family:arial, helvetica, clean, sans-serif;} #ygrp-mlmsg table {font-size:inherit;font:100%;} #ygrp-mlmsg select, input, textarea {font:99% arial, helvetica, clean, sans-serif;} #ygrp-mlmsg pre, code {font:115% monospace;} #ygrp-mlmsg * {line-height:1.22em;} #ygrp-text{ font-family:Georgia; } #ygrp-text p{ margin:0 0 1em 0;} #ygrp-tpmsgs{ font-family:Arial; clear:both;} #ygrp-vitnav{ padding-top:10px;font-family:Verdana;font-size:77%;margin:0;} #ygrp-vitnav a{ padding:0 1px;} #ygrp-actbar{ clear:both;margin:25px 0;white-space:nowrap;color:#666;text-align:right;} #ygrp-actbar .left{ float:left;white-space:nowrap;} ...bld{font-weight:bold;} #ygrp-grft{ font-family:Verdana;font-size:77%;padding:15px 0;} #ygrp-ft{ font-family:verdana;font-size:77%;border-top:1px solid #666; padding:5px 0; } #ygrp-mlmsg #logo{ padding-bottom:10px;} #ygrp-vital{ background-color:#e0ecee;margin-bottom:20px;padding:2px 0 8px 8px;} #ygrp-vital #vithd{ font-size:77%;font-family:Verdana;font-weight:bold;color:#333;text-transform:upp\ ercase;} #ygrp-vital ul{ padding:0;margin:2px 0;} #ygrp-vital ul li{ list-style-type:none;clear:both;border:1px solid #e0ecee; } #ygrp-vital ul li .ct{ font-weight:bold;color:#ff7900;float:right;width:2em;text-align:right;padding-ri\ ght:.5em;} #ygrp-vital ul li .cat{ font-weight:bold;} #ygrp-vital a{ text-decoration:none;} #ygrp-vital a:hover{ text-decoration:underline;} #ygrp-sponsor #hd{ color:#999;font-size:77%;} #ygrp-sponsor #ov{ padding:6px 13px;background-color:#e0ecee;margin-bottom:20px;} #ygrp-sponsor #ov ul{ padding:0 0 0 8px;margin:0;} #ygrp-sponsor #ov li{ list-style-type:square;padding:6px 0;font-size:77%;} #ygrp-sponsor #ov li a{ text-decoration:none;font-size:130%;} #ygrp-sponsor #nc{ background-color:#eee;margin-bottom:20px;padding:0 8px;} #ygrp-sponsor .ad{ padding:8px 0;} #ygrp-sponsor .ad #hd1{ font-family:Arial;font-weight:bold;color:#628c2a;font-size:100%;line-height:122%\ ;} #ygrp-sponsor .ad a{ text-decoration:none;} #ygrp-sponsor .ad a:hover{ text-decoration:underline;} #ygrp-sponsor .ad p{ margin:0;} o{font-size:0;} ...MsoNormal{ margin:0 0 0 0;} #ygrp-text tt{ font-size:120%;} blockquote{margin:0 0 0 4px;} ...replbq{margin:4;} --> ________________________________________________________________________________\ ____ Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. http://mobile.yahoo.com/;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2008 Report Share Posted March 11, 2008 Hi Loretta, Thanks for the " snapping " info. As soon as I find a doctor that is interested in fibro, I will find out!!!! Gentle hug back! /Mi Re: Snapping muscles????!!!! Hello , My left arm has a muscle that snaps sometimes. It hurts. I think for me at least it's the Myofascial pain syndrome. Have you looked into that? SOmetimes the fascia can become hard and kind of bind the muscles in to a certain position, then when you move the muscle, it seems to snap it... gentle hugs, Loretta > > Hi all, > Has anyone experienced this weird thing: sometimes when I turn the > muscles in the front of my thighs feel almost like they snap and the > pain when this happens is excruciating. Also, my symptoms seem to be a > bit more pronounced on one side of my body than the other...is this > unheard of???? My sister in law has MS and she said my symptoms sounded > like hers before she was diagnosed. I was like " gee, thanks!! " . > Thanks for any input. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2008 Report Share Posted March 12, 2008 Listmates, These conversations about lumps and such seem so relevant to what I'm hearing about. One of my listmates on the low oxalate list who has fibromyalgia said: >Hi I am new here and have been on the LOD (low oxalate diet) >for a little over a month after being GFDF (gluten and dairy free)for almost >two years. I have fibromyalgia and severe gluten intolerance. The results >have been astonishing for me with incredible improvements. I am literally >dissolving! I was wondering if there is any kind of damage/danger in sudden > shedding of oxalates in tissue?.... The hard painful lumps and sharp pains > in my feet and legs are gone, as >well as fibrocystic breast lumps and hardened painful chest wall >lumps. Any advice or experiences with this would be so welcome. I feel >very excited, yet alone in this whole experience, as any of the doctors >I have talked to know nothing about this. What she said makes sense because, literally, oxalates bind minerals (especially calcium) and crystallize in tissues. If that is what is making these tissues stiff so that they snap, reducing oxalates might improve this condition. Before I reduced oxalates in myself, I would find that I would start to " pop " in the joints of my feet (probably more ankles) when I had a few days of higher oxalates. This always happened when I was travelling and eating in hotel restaurants, and that popping would be embarrassingly loud when I walked down those long hotel hallways and it would get louder and more obvious the more I ate those hotel high-oxalate salads and more potatoes than usual. (The " field green " salads must be extraordinarily high in oxalate.) One of my biggest shocks was after about two weeks on this diet, I had a surge in energy and could suddenly walk and go up stairs at several times my previous speed. I had started to walk like an old woman. Others have described this change, too. In fact this last week, I talked to a 75 year old woman I have known for thirteen years. In the last two years, she has lowered oxalates for the benefit of her 46 year old son with autism. His changes have been extraordinary...His speech has improved, he is picking up self-help skills he never had, and he is now curious, and she is having to " baby-proof " her home because he is now getting into things he never noticed before. She is just as excited to talk about changes she's seen in herself in the reduction of arthritic pain and stiffness. She said her doctor was astonished at how much less stiff she was when she came in recently for her annual physical. The change was dramatic enough that the doctor was really quizzing her about what she'd changed. Especially because of the pain angle, I just don't want people to miss the opportunity of trying this just because it sounds weird for a diet to change so much. It really DOES make a big difference in some people and it doesn't take long AT ALL to figure out if the diet is doing anything. Usually most people see changes in a few days to a week....hardly a big commitment! -- In <mailto:Fibromyalgia_Support_Group%40yahoogroups.com>Fibromyalgia_Support_Group@\ yahoogroups.com, " uniceander " > wrote: > > > > Hi all, > > Has anyone experienced this weird thing: sometimes when I turn the > > muscles in the front of my thighs feel almost like they snap and the > > pain when this happens is excruciating. Also, my symptoms seem to be a > > bit more pronounced on one side of my body than the other...is this > > unheard of???? My sister in law has MS and she said my symptoms sounded > > like hers before she was diagnosed. I was like " gee, thanks!! " . > > Thanks for any input. > > > > > > -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.5.516 / Virus Database: 269.21.6/1316 - Release Date: 3/6/2008 6:58 PM Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2008 Report Share Posted March 12, 2008 Hi - I have heard from more than one source now that gluten free diets have helped them a lot and their symptoms and pain are less since they have been on it. I am wondering since I have been doing low carbs (the only gluten I get now is from 2 slices of low carb bread I fondly call " air bread " a day, 4 days a week) and have felt so much better, if it's not due, in part, from the drastic reduction in gluten products myself. I have had very little pasta and/or rice since last October. Only once in awhile if I am at my kid's house and they have a cassarole. Wonder if that could be it (in addition to the Lyrica). Owens wrote: Listmates, These conversations about lumps and such seem so relevant to what I'm hearing about. One of my listmates on the low oxalate list who has fibromyalgia said: >Hi I am new here and have been on the LOD (low oxalate diet) >for a little over a month after being GFDF (gluten and dairy free)for almost >two years. I have fibromyalgia and severe gluten intolerance. The results >have been astonishing for me with incredible improvements. I am literally >dissolving! I was wondering if there is any kind of damage/danger in sudden > shedding of oxalates in tissue?.... The hard painful lumps and sharp pains > in my feet and legs are gone, as >well as fibrocystic breast lumps and hardened painful chest wall >lumps. Any advice or experiences with this would be so welcome. --------------------------------- Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2008 Report Share Posted March 12, 2008 , There is an immune factor called zonulin that opens up the " leaky gut " when exposed to gluten in the GI tract. That happens to everybody, but is worse with those with celiac disease, and hasn't been measured yet, as far as I can tell, in other conditions. If you don't open up the " leaky gut " then oxalates stop being as big a problem. Also, a history of antibiotics can be a problem because they destroy the oxalate-degrading microbes that are in the colon. So, yes, it might make a difference if you became a " t-totaler " on the gluten and avoid high oxalate foods as well. Anything that contains gluten is also high oxalate. You have to be careful if you use substitute grains, however, as many of them are higher in oxalate than wheat. At 03:47 PM 3/12/2008, you wrote: >Hi - I have heard from more than one source now that gluten free >diets have helped them a lot and their symptoms and pain are less since >they have been on it. I am wondering since I have been doing low carbs >(the only gluten I get now is from 2 slices of low carb bread I fondly >call " air bread " a day, 4 days a week) and have felt so much better, if >it's not due, in part, from the drastic reduction in gluten products >myself. I have had very little pasta and/or rice since last October. Only >once in awhile if I am at my kid's house and they have a cassarole. Wonder >if that could be it (in addition to the Lyrica). > > > > Owens wrote: >Listmates, > >These conversations about lumps and such seem so relevant to what I'm >hearing about. >One of my listmates on the low oxalate list who has fibromyalgia said: > > >Hi I am new here and have been on the LOD (low oxalate diet) > >for a little over a month after being GFDF (gluten and dairy free)for almost > >two years. I have fibromyalgia and severe gluten intolerance. The results > >have been astonishing for me with incredible improvements. I am literally > >dissolving! I was wondering if there is any kind of damage/danger in sudden > > shedding of oxalates in tissue?.... The hard painful lumps and sharp pains > > in my feet and legs are gone, as > >well as fibrocystic breast lumps and hardened painful chest wall > >lumps. Any advice or experiences with this would be so welcome. > >--------------------------------- >Be a better friend, newshound, and know-it-all with Yahoo! Mobile. Try it now. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2008 Report Share Posted March 12, 2008 , I must look into this low oxalate thing...very interesting, thanks! /Mi Re: Re: Snapping muscles????!!!! Listmates, These conversations about lumps and such seem so relevant to what I'm hearing about. One of my listmates on the low oxalate list who has fibromyalgia said: >Hi I am new here and have been on the LOD (low oxalate diet) >for a little over a month after being GFDF (gluten and dairy free)for almost >two years. I have fibromyalgia and severe gluten intolerance. The results >have been astonishing for me with incredible improvements. I am literally >dissolving! I was wondering if there is any kind of damage/danger in sudden > shedding of oxalates in tissue?.... The hard painful lumps and sharp pains > in my feet and legs are gone, as >well as fibrocystic breast lumps and hardened painful chest wall >lumps. Any advice or experiences with this would be so welcome. I feel >very excited, yet alone in this whole experience, as any of the doctors >I have talked to know nothing about this. What she said makes sense because, literally, oxalates bind minerals (especially calcium) and crystallize in tissues. If that is what is making these tissues stiff so that they snap, reducing oxalates might improve this condition. Before I reduced oxalates in myself, I would find that I would start to " pop " in the joints of my feet (probably more ankles) when I had a few days of higher oxalates. This always happened when I was travelling and eating in hotel restaurants, and that popping would be embarrassingly loud when I walked down those long hotel hallways and it would get louder and more obvious the more I ate those hotel high-oxalate salads and more potatoes than usual. (The " field green " salads must be extraordinarily high in oxalate.) One of my biggest shocks was after about two weeks on this diet, I had a surge in energy and could suddenly walk and go up stairs at several times my previous speed. I had started to walk like an old woman. Others have described this change, too. In fact this last week, I talked to a 75 year old woman I have known for thirteen years. In the last two years, she has lowered oxalates for the benefit of her 46 year old son with autism. His changes have been extraordinary...His speech has improved, he is picking up self-help skills he never had, and he is now curious, and she is having to " baby-proof " her home because he is now getting into things he never noticed before. She is just as excited to talk about changes she's seen in herself in the reduction of arthritic pain and stiffness. She said her doctor was astonished at how much less stiff she was when she came in recently for her annual physical. The change was dramatic enough that the doctor was really quizzing her about what she'd changed. Especially because of the pain angle, I just don't want people to miss the opportunity of trying this just because it sounds weird for a diet to change so much. It really DOES make a big difference in some people and it doesn't take long AT ALL to figure out if the diet is doing anything. Usually most people see changes in a few days to a week....hardly a big commitment! -- In <mailto:Fibromyalgia_Support_Group%40yahoogroups.com>Fibromyalgia_Support_Group@\ yahoogroups.com, " uniceander " > wrote: > > > > Hi all, > > Has anyone experienced this weird thing: sometimes when I turn the > > muscles in the front of my thighs feel almost like they snap and the > > pain when this happens is excruciating. Also, my symptoms seem to be a > > bit more pronounced on one side of my body than the other...is this > > unheard of???? My sister in law has MS and she said my symptoms sounded > > like hers before she was diagnosed. I was like " gee, thanks!! " . > > Thanks for any input. > > > > > > -- No virus found in this outgoing message. Checked by AVG Free Edition. Version: 7.5.516 / Virus Database: 269.21.6/1316 - Release Date: 3/6/2008 6:58 PM Quote Link to comment Share on other sites More sharing options...
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